Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707895Generated: November 1, 2026

2-Methyl-3-butyn-2-ol → 4-(4-Butylphenyl)-2-methyl-3-butyn-2-ol

https://huagongshe.com/reaction/1707895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
Reactant1-Bromo-4-butylbenzeneHCID 521059—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product4-(4-Butylphenyl)-2-methyl-3-butyn-2-olHCID 1895999441.9%

Reaction Steps

1-Bromo-4-butylbenzene (235 g), 3-methyl-1-butyne-3-ol (139 g), triphenylphosphine (4.8 g) and bis(triphenylphosphine)palladium(II) chloride (2.8 g) were dissolved in triethylamine (1,000 ml), and then copper(I) iodide (0.8 g) was added thereto. After stirring at room temperature for 1 hour, the reaction mixture was further stirred at 90° C. for 5 hours. The resulting precipitated crystals were filtered, and then triethylamine was distilled off therefrom, followed by extracting with chloroform. The resultant was washed with 10% hydrochloric acid twice, and further with water twice, and then chloroform was distilled off therefrom. The residue was purified using silica gel-chloroform column chromatography to give 3-methyl-1-(4'-butylphenyl)-1-butyne-3-ol (100 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356558
Source datasetuspto-grants-1994_10
ORD IDord-f4b09eafe8e443e4a4295089bb11db65
Source noteuspto-grants-1994_10